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    WHCR Wolf-Hirschhorn syndrome chromosome region [ Homo sapiens (human) ]

    Gene ID: 7467, updated on 10-Apr-2021

    Summary

    Gene symbol
    WHCR
    Gene description
    Wolf-Hirschhorn syndrome chromosome region
    Primary source
    MIM:194190
    Gene type
    other
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    PRDS
    Summary
    Wolf-Hirschhorn syndrome is a congenital malformation syndrome characterized by pre- and postnatal growth deficiency, developmental disability of variable degree, characteristic craniofacial features ('Greek warrior helmet' appearance of the nose, high forehead, prominent glabella, hypertelorism, high-arched eyebrows, protruding eyes, epicanthal folds, short philtrum, distinct mouth with downturned corners, and micrognathia), and a seizure disorder (Battaglia et al., 2008 [PubMed 18932224]).[supplied by OMIM, Nov 2010]
    Annotation information
    not in current annotation release
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